1. A CGG‐Repeat Expansion Mutation in ZNF713 Causes FRA7A: Association with Autistic Spectrum Disorder in Two Families. Issue 11 (November 2014) Authors: Metsu, Sofie; Rainger, Jacqueline K.; Debacker, Kim; Bernhard, Birgitta; Rooms, Liesbeth; Grafodatskaya, Daria; Weksberg, Rosanna; Fombonne, Eric; Taylor, Martin S.; Scherer, Stephen W.; Kooy, R. Frank; FitzPatrick, David R. Journal: Human mutation Issue: Volume 35:Issue 11(2014:Nov.) Page Start: 1295 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage. Issue 5 (2nd May 2007) Authors: Debacker, Kim; Winnepenninckx, Birgitta; Ben-Porat, Neta; FitzPatrick, David; Van Luijk, Rob; Scheers, Stefaan; Kerem, Batsheva; Frank Kooy, R Journal: Journal of medical genetics Issue: Volume 44:Issue 5(2007) Page Start: 347 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗